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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375685Generated: October 26, 2026

Triethylamine → 4-Tert-butyl 3-ethyl 5-(3-iodophenyl)isoxazole-3,4-dicarboxylate

https://huagongshe.com/reaction/1375685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-chloro-2-(hydroxyimino)acetateHCID 6399471—
ReactantTert-butyl 3-(3-iodophenyl)-3-oxopropanoateHCID 69508156—
SolventEthanolHCID 702—
Product4-Tert-butyl 3-ethyl 5-(3-iodophenyl)isoxazole-3,4-dicarboxylateHCID 6950822635.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl 3-(3-iodophenyl)-3-oxopropanoate (1.91 g, 5.52 mmol) was dissolved in ethanol (6 mL), cooled to 0° C., and Et3N (558 mg, 5.52 mmol) was added. After stirring 20 minutes, ethyl chlorooximidoacetate (836 mg, 5.52 mmol) in EtOH (3 mL) was added to the reaction mixture over 30 min. The reaction mixture was warmed to ambient temperature and stirred overnight. The mixture was concentrated in vacuo and purified by column chromatography (0–13% ethyl acetate in hexanes) to provide the titled compound (860 mg, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169797B2
Source datasetuspto-grants-2007_01
ORD IDord-c22ad55f1beb4683a358d43599c40d90
Source noteuspto-grants-2007_01